TMPRSS12 anticorps (N-Term)

N° du produit ABIN1539224

L’anticorps Lapin Polyclonal anti-TMPRSS12 a été validé pour WB. Il convient pour détecter TMPRSS12 dans des échantillons de Humain.

Aperçu rapide pour TMPRSS12 anticorps (N-Term) (ABIN1539224)

Antigène: TMPRSS12 (Transmembrane (C-terminal) Protease, serine 12 (TMPRSS12))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMPRSS12 est non-conjugé

Application: Western Blotting (WB)

Clone: RB35931

Détail du produit anti-TMPRSS12 anticorps

Épitope: AA 26-54, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This TMPRSS12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 26-54 amino acids from the N-terminal region of human TMPRSS12.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: TMPRSS12 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur TMPRSS12

Antigène: TMPRSS12 (Transmembrane (C-terminal) Protease, serine 12 (TMPRSS12))

Autre désignation: TMPRSS12

Sujet: TMPRSS12 (transmembrane protease serine 12) is a 348 amino acid single-pass membrane protein that belong to the peptidase S1 family and contains one peptidase S1 domain. The gene that encodes TMPRSS12 consists of nearly 45,000 bases and maps to human chromosome 12q13.12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster, encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms which vary in severity depending on the extent of mosaicism.

Poids moléculaire: 38605

ID gène: 283471

NCBI Accession: NP_872365

UniProt: Q86WS5